Evidence map›Paper›PMID 23342261›Full record

ArticleCancer medicine2012

Heterogeneity of breast cancer stem cells as evidenced with Notch-dependent and Notch-independent populations.

Nelson K Y Wong, Megan Fuller, Sandy Sung, Fred Wong, Aly Karsan

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  3. Heterogeneity of BCSCs contributes to the metastatic organotropism of breast cancer.Journal of experimental & clinical cancer research : CR · 2021
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  16. Breast cancer stem cells.Frontiers in physiology · 2013
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Nelson K Y WongGenome Sciences Centre, BC Cancer Agency Vancouver, BC, Canada; Department of Pathology and Laboratory Medicine, University of British Columbia Vancouver, BC, Canada.
Megan Fuller
Sandy Sung
Fred Wong
Aly Karsan
BC Cancer Agency · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies have suggested the potential importance of Notch signaling to the cancer stem cell population in some tumors, but it is not known whether all cells in the cancer stem cell fraction require Notch activity. To address this issue, we blocked Notch activity in MCF-7 cells by expressing a dominant-negative MAML-GFP (dnMAML) construct, which inhibits signaling through all Notch receptors, and quantified the effect on tumor-initiating activity. Inhibition of Notch signaling reduced primary tumor sphere formation and side population. Functional quantification of tumor-initiating cell numbers in vivo showed a significant decrease, but not a complete abrogation, of these cells in dnMAML-expressing cells. Interestingly, when assessed in secondary assays in vitro or in vivo, there was no difference in tumor-initiating activity between the dnMAML-expressing cells and control cells. The fact that a subpopulation of dnMAML-expressing cells was capable of forming primary and secondary tumors indicates that there are Notch-independent tumor-initiating cells in the breast cancer cell line MCF-7. Our findings thus provide direct evidence for a heterogeneous cancer stem cell pool, which will require combination therapies against multiple oncogenic pathways to eliminate the tumor-initiating cell population.

Indexed as

AnimalsBreast NeoplasmsCarcinogenesisCD24 AntigenCell Line, TumorCell ProliferationDNA-Binding ProteinsFemaleGreen Fluorescent ProteinsHumansHyaluronan ReceptorsIntegrin alpha6MCF-7 CellsMiceMice, Inbred NODMice, SCIDCD24 AntigenDNA-Binding ProteinsGreen Fluorescent ProteinsHyaluronan ReceptorsIntegrin alpha6MAML1 protein, humanReceptors, NotchTranscription FactorsBreast cancercancer stem cellsdominant-negative MAMLMCF-7Notch

Identifiers

PMID23342261
PMCPMC3544441
OpenAlexW1979004607

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.